FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 2893604 · Received January 2, 2013

Report

Report Number
9616091-2013-00002
Event Type
Malfunction
Date Received
January 2, 2013
Report Date
January 1, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER STATES CROSSBRACE BROKEN. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
300 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9SL

Patients

Seq Age Sex Outcome Treatment
1 Other